共 27 条
Survivin as a global target of intrinsic tumor suppression networks
被引:125
作者:

Guha, Minakshi
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Massachusetts, Sch Med, Dept Canc Biol, Worcester, MA 01605 USA Univ Massachusetts, Sch Med, Dept Canc Biol, Worcester, MA 01605 USA

Altieri, Dario C.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Massachusetts, Sch Med, Dept Canc Biol, Worcester, MA 01605 USA Univ Massachusetts, Sch Med, Dept Canc Biol, Worcester, MA 01605 USA
机构:
[1] Univ Massachusetts, Sch Med, Dept Canc Biol, Worcester, MA 01605 USA
来源:
关键词:
survivin;
PTEN;
tumor suppressor;
apoptosis;
gene regulation;
WILD-TYPE P53;
ANTITUMOR-ACTIVITY;
GENE-EXPRESSION;
BREAST-CANCER;
APOPTOSIS;
PATHWAY;
REPRESSION;
INHIBITOR;
THERAPY;
MITOSIS;
D O I:
10.4161/cc.8.17.9457
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Despite the constant exposure to genomic insults that may lead to malignancy, cancer is surprisingly a relatively rare occurrence, and this is largely credited to an elaborate network of endogenous tumor suppression. Many effectors of tumor suppression have been identified, and their functions when activated in damaged cells have in large part been elucidated. What is less clear is whether there are common target gene(s) of tumor suppression, whose expression must be ablated in order to block transformation and preserve cellular homeostasis. Fresh experimental evidence suggests that silencing of the mitotic regulator and cell death inhibitor, survivin, is a universal requirement for successful tumor suppression in humans.
引用
收藏
页码:2708 / 2710
页数:3
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